Canonical Allele Identifier:
CA261186143
Gene:
Linked Data
dbSNP Id:
rs991335033
gnomAD v3:
14-49067756-C-A
gnomAD v4:
14-49067756-C-A
MyVariant Identifiers:
chr14:g.49067756C>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.49067756C>A , CM000676.2:g.49067756C>A | GRCh38 |
| NC_000014.8:g.49534474C>A , CM000676.1:g.49534474C>A | GRCh37 |
| NC_000014.7:g.48604224C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943837.1:n.222+2036G>T | ||
| XR_943837.2:n.345+2036G>T |